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HRID 555792作成日:2026年10月27日

Hydrochloric Acid → (4-(3-chloropyrazin-2-yloxy)phenyl)(1H-benzo[d]imidazol-2-yl)methanone

https://huagongshe.com/reaction/555792

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物O-PhenylenediamineHCID 7243—
反応物Benzenesulfonic AcidHCID 7371—
反応物Sodium HydroxideHCID 14798—
反応物Ethyl orthoformateHCID 31214—
反応物Lithium diisopropylamideHCID 2724682—
反応物Ethyl 4-[(3-chloropyrazin-2-yl)oxy]benzoateHCID 45031059—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物(4-(3-chloropyrazin-2-yloxy)phenyl)(1H-benzo[d]imidazol-2-yl)methanoneHCID 46207940—

反応手順

A solution of benzene-1,2-diamine (1.5 g, 14 mmol), triethyl orthoformate (5.7 mL, 37 mmol), and benzenesulfonic acid (0.075 g, 0.47 mmol) in toluene (15 mL) was heated to reflux for 4 h and then slowly distilled to remove half of the solvent. The mixture was then cooled to RT and neutralized with diisopropyl amine, followed by addition of a solution of ethyl 4-(3-chloropyrazin-2-yloxy)benzoate (4.3 g, 15 mmol) in THF (15 mL). The mixture was cooled to −78° C. and 1.2 equiv of LDA (9.2 mL, 17 mmol) was added. After aging at −78° C. for 1.5 h, the mixture was warmed to RT after 1.5 h and then 2N HCl was added and the mixture was agitated for 30 min. Following that, the mixture was adjusted to pH 9 with 1N NaOH. Ethyl acetate was added and the layers were separated, the aqueous was extracted with ethyl acetate (3×), and the combined organics were washed with brine, dried over Na2SO4, filtered and concentrated. Upon treatment with MeOH, a yellow solid crashed out which was filtered and collected to give (1H-benzo[d]imidazol-2-yl)(4-(3-chloropyrazin-2-yloxy)phenyl)methanone.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08053438B2
出典データセットuspto-grants-2011_11
ORD IDord-377fce8bcbc243d483d3f6e5c2289810
出典メモuspto-grants-2011_11